Pages that link to "Q28248365"
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The following pages link to Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1 (Q28248365):
Displaying 50 items.
- acromesomelic dysplasia, Grebe type (Q9190289) (← links)
- Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size (Q21092465) (← links)
- Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis (Q22009041) (← links)
- Human disease-causing NOG missense mutations: effects on noggin secretion, dimer formation, and bone morphogenetic protein binding (Q24291700) (← links)
- Systemically administered bone morphogenetic protein-6 restores bone in aged ovariectomized rats by increasing bone formation and suppressing bone resorption (Q24294642) (← links)
- Zinc-finger protein 145, acting as an upstream regulator of SOX9, improves the differentiation potential of human mesenchymal stem cells for cartilage regeneration and repair (Q24301561) (← links)
- Crystal structure analysis reveals a spring-loaded latch as molecular mechanism for GDF-5-type I receptor specificity (Q24312827) (← links)
- Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2 (Q24318483) (← links)
- A GDF5 point mutation strikes twice--causing BDA1 and SYNS2 (Q24337747) (← links)
- Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene (Q24533489) (← links)
- The role of growth/differentiation factor 5 (GDF5) in the induction and survival of midbrain dopaminergic neurones: relevance to Parkinson's disease treatment (Q24675617) (← links)
- Robinow syndrome (Q24679335) (← links)
- Interplay between bone morphogenetic proteins and cognate binding proteins in bone and cartilage development: noggin, chordin and DAN. (Q24805190) (← links)
- TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease (Q26738766) (← links)
- Targets, models and challenges in osteoarthritis research (Q26850147) (← links)
- TGFbeta signaling in growth control, cancer, and heritable disorders (Q28142605) (← links)
- Wnt-14 plays a pivotal role in inducing synovial joint formation in the developing appendicular skeleton (Q28203665) (← links)
- Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes (Q28212192) (← links)
- Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome) (Q28214855) (← links)
- Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia (Q28215079) (← links)
- Effect of intracellular interactions on the processing and secretion of bone morphogenetic protein-15 (BMP-15) and growth and differentiation factor-9. Implication of the aberrant ovarian phenotype of BMP-15 mutant sheep (Q28215801) (← links)
- Functional and molecular characterization of naturally occurring mutations in the oocyte-secreted factors bone morphogenetic protein-15 and growth and differentiation factor-9 (Q28245670) (← links)
- Mutations in CDMP1 cause autosomal dominant brachydactyly type C (Q28248352) (← links)
- Adams-Oliver syndrome: Additions to the clinical features and possible role of BMP pathway (Q28252125) (← links)
- Bone morphogenetic protein type IA receptor signaling regulates postnatal osteoblast function and bone remodeling (Q28257036) (← links)
- Cartilage-derived morphogenetic protein-1 (Q28260644) (← links)
- Missense mutations in the BMP15 gene are associated with ovarian failure (Q28299705) (← links)
- Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes (Q28306123) (← links)
- Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN (Q28587807) (← links)
- Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe (Q28588639) (← links)
- Developmental failure of phalanges in the absence of growth/differentiation factor 5 (Q28589484) (← links)
- Amino acid 72 of mouse and human GDF9 mature domain is responsible for altered homodimer bioactivities but has subtle effects on GDF9:BMP15 heterodimer activities (Q28591841) (← links)
- Role of CDMP-1 in skeletal morphogenesis: promotion of mesenchymal cell recruitment and chondrocyte differentiation (Q28594745) (← links)
- A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia (Q28647893) (← links)
- GDF-5 deficiency in mice leads to disruption of tail tendon form and function (Q30309116) (← links)
- Grebe syndrome in Vietnamese sisters: not Agent Orange (Q31894627) (← links)
- A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family (Q33387662) (← links)
- Growth Differentiation Factor 5-Mediated Enhancement of Chondrocyte Phenotype Is Inhibited by Heparin: Implications for the Use of Heparin in the Clinic and in Tissue Engineering Applications (Q33580590) (← links)
- A consistent and potentially exploitable response during chondrogenesis of mesenchymal stem cells from osteoarthritis patients to the protein encoded by the susceptibility gene GDF5 (Q33648169) (← links)
- A general approach for identifying distant regulatory elements applied to the Gdf6 gene (Q33679006) (← links)
- Grebe syndrome: a second case with extremely severe manifestations (Q33679960) (← links)
- Genetics of limb anomalies in humans (Q33739354) (← links)
- Actions of hedgehog proteins on skeletal cells (Q33817061) (← links)
- Genetic approaches to TGFbeta signaling pathways (Q33824603) (← links)
- The Good the Bad and the Ugly of Glycosaminoglycans in Tissue Engineering Applications (Q33851544) (← links)
- Genetic disorders of the skeleton: a developmental approach (Q33906292) (← links)
- Gene expression analysis suggests bone development-related genes GDF5 and DIO2 are involved in the development of Kashin-Beck disease in children rather than adults (Q33968546) (← links)
- Changes in clinical practice with the unravelling of diseases: connective-tissue disorders (Q34280965) (← links)
- Transforming growth factor beta signalling in vitro and in vivo: activin ligand-receptor interaction, Smad5 in vasculogenesis, and repression of target genes by the deltaEF1/ZEB-related SIP1 in the vertebrate embryo. (Q34307632) (← links)
- Positive selection on the osteoarthritis-risk and decreased-height associated variants at the GDF5 gene in East Asians (Q34384481) (← links)